Customized surgical guides, methods for manufacturing and uses thereof

ABSTRACT

The invention relates to surgical guides which are of use during reconstructive bone surgery for guiding a surgical instrument or tool. More particularly, the guides are characterized in that they are fitted to the implant rather than to the bone.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part of U.S. application Ser. No.13/515,141, filed Jun. 11, 2012, which is a U.S. national phase of PCTApplication No. PCT/EP2010/070777, filed Dec. 28, 2010, which claimspriority to U.S. Provisional Application No. 61/290,673, filed Dec. 29,2009 and Great Britain Application No. 0922640.8, filed Dec. 29, 2009,the contents of which are hereby incorporated by reference.

FIELD OF THE INVENTION

The present invention relates to surgical guides which are of use duringreconstructive bone surgery, more specifically during reconstructivejoint surgery, for guiding a surgical instrument or tool. The presentinvention further relates to methods for manufacturing these surgicalguides and specific methods for using the surgical guides of theinvention in reconstructive bone and joint surgery.

BACKGROUND

In most bone or joint arthroplasty, replacement and/or reconstructionsurgery procedures, a bone or a joint is replaced by a prostheticimplant. The main goal of an arthroplasty intervention is to relieve(arthritis) pain or to restore severe physical joint damage resultingfrom, for example, trauma. When a prosthesis fails, a revisionarthroplasty is carried out. This procedure is technically moredifficult and time-consuming than the primary intervention and theoutcome is often less satisfactory, both because there is less bonestock to work with and because the removal of adherent cement orprosthetic components may result in fracture or perforation of the bone.With each successive joint revision, the risk of infection andsymptomatic loosening of the prosthesis may increase substantially.Revision surgeries become more frequent as the population grows olderand patients receive prostheses at an earlier age.

The treatment of bone and joint defects has gradually become morecomplex. While it started out with standard interventions usingoff-the-shelf prosthesis components, it has evolved to patient-specificsurgery plans and patient-specific implant designs. The accurate andstable fixation of implants onto the bone or joint, while increasinglydifficult, remains one of the most important steps in arthroplastyinterventions.

The standard process of fixing or anchoring an implant with screws intothe bone is mostly a two-step procedure. First, the screw trajectory ispre-drilled with a dedicated instrument. This is followed by the screwinsertion along the pre-drilled screw trajectory. Some self-tappingscrew types do not require pre-drilling; direct insertion of the screw,directly establishes the screw trajectory.

Unfortunately, this anchoring process has a number of importantdrawbacks.

Indeed, deviations in direction and/or location of the screw trajectoryoften lead to a suboptimal screw traction which may cause soft tissuedamage. The pre-drilling and/or placing of the screws are often done bythe surgeon free-hand style, with only a limited view on the bonethrough the available surgical incision. Moreover, where the surgeon hassufficient exposure of the patient and a wide view on the implant andscrew hole and is able to orient the pre-drilling instrument in anyorientation (which is not often the case), he will typically use thesurface curvature of the implant around the screw hole as a visualreference and will aim at placing the instrument orthogonally withrespect to the local implant surface. As a result, the obtained screwdirections are often suboptimal and/or deviate from a preoperative plan.Screws can for example be directed in bone of low quality, or have onlylimited traction length. In addition, a shift of the implant away fromthe optimal location before pre-drilling has started can cause screwlocations, i.e. insertion points of the screw trajectories into thebone, to deviate from a predetermined location.

Deviations in the direction and/or location of a screw trajectory mayalso cause the screws to become mutually intersecting, causing e.g. theinsertion of a first screw (either with or without a planned direction)to block the insertion of the next. Unused screw holes badly influencethe implant's long-term integrity, unless some other portion of theimplant compensates the local decrease in material volume. This howeverimplies the use of more implant material, for example thickening of theimplant, making it more bulky, and/or requires larger contact regionswith the bone. The latter again is detrimental to soft tissuepreservation.

Specific tools and technologies have been developed in the past in orderto solve the above problems associated with the fixation or anchoringprocess of the implant.

Navigation technology has for instance been used as a global positioningsystem for the surgeon. For example, infrared sensors placed near thebone or joint in the operating room act like satellites constantlymonitoring the location of markers and instruments placed along apatient's anatomy. Unfortunately, this technology is expensive andintra-operatively very time-consuming.

A system for fixation of an implant onto a bone is provided in U.S. Pat.No. 7,153,309 (Huebner et al.), in which a guide device is attached to abone plate. The use of this device is in practice however limited toanatomical areas which can be extensively exposed or can be easilyapproached from different directions. For example, the device does notallow pre-drilling from the ipsilateral side of a bone plate, aprocedure which is however often needed, for example in implant surgeryof the hemi-pelvis, scapula, or mandible. US2008/0183172 describes aguide for a bone plate which is more compact but similarly comprises aprojection extending from the guide which is configured to be receivedwithin an aperture in the bone plate for securing the plate guide to theplate. The aperture can be a bone-screw receiving aperture inherentlypresent on existing bone plates or an aperture designed to receive aprojection comprising a resilient finger. These devices can however onlybe applied in cases of bone repair (following traumata, with multiplebone fragments), and not for bone and joint repair such as inarthroplasty. In addition, the described plate-guide fixation systemsdefine the direction and insertion point of a connective feature withrespect to the plate, and (only if the plate is patient-specific) alsowith respect to the bone. Accordingly, absolute referencing, needed totransfer a preoperative surgery plan on the patient bone geometry andderived from medical images onto the patient's bone during surgery, isnot guaranteed. Finally, the guides are physically attached to theplate, requiring attachment features on both components and moreoverrequiring assembly manipulations.

Standard-size drill guiding cylinders have been described, which can bescrewed into the implant screw hole (such as for example for theCompliant Pre-Stress (CPS) device of Biomet Inc.; Warsaw, Ind.). Due toreasons of manufacturability, machine set-up time and costs, thisguiding solution is limited to large series of off-the-shelf implants,for which it is economically profitable to set up expensive threadingmachinery.

Patient-specific bone guides have a unique (partial) fit with a portionof the surrounding bone, and therefore allow the guiding of features,such as bone drilling and/or cutting elements, in an unambiguous andaccurately planned trajectory or direction into the bone (Tardieu PB(2007) Int. J. Periodontics Restorative Dent. 27(2): 141-149; Kunz M(2007) Proceedings of the 7^(th) Annual Meeting of CAOS-International:159-161; Lombardi Jr AV et al. (2008) BFA Orthopedics; 31: 927).However, a custom bone guide is not always a guarantee for adequateimplant fixation, especially in the case of a patient-specific implant.For certain anatomical regions, and especially in complex revisioncases, the only bone regions which can be exposed and reached throughthe surgical window are few, small and spread out. One could think of apatient-specific implant reaching out to these regions for fixation.Pre-drilling screw holes could be performed with a plastic implantreplica serving as a base frame for the bone guides. This is howeverunpractical and ineffective since the guide-frame construction has to betaken out, and the implant reinserted while keeping track of thepre-drill locations. Furthermore, the use of a Kirschner wire to keeptrack of the pre-drill locations while sliding off the guide and slidingthe implant on is not convenient and not fully constrained.

Accordingly, there is a need for alternative and improved (customized)surgical guides, which are stable and which provide the ability toaccurately insert a surgical instrument into a patient's bone or joint.

SUMMARY OF THE INVENTION

The present invention relates to customized surgical guides forpatient-specific bone implants, which ensure a stable guidance of thesurgical instrument into the bone as well as an accurate fixation of thebone implant. Instead of being mounted onto one or more patient-specificsurfaces of the bone, as in surgical bone guides, the guides accordingto the present invention are directly positioned onto the finalpatient-specific bone implant. This is ensured by a specific fit betweenthe customized surgical guide and the bone implant. In particularembodiments this is ensured by specific fit between surface structuresof the customized surgical guide and one or more surface structures ofthe patient-specific bone implant. Additionally or alternatively this isensured by the patient-specific localization and orientation of lockingfeatures and/or guiding elements provided on the surgical guide. Uponusing the customized surgical guides according to the invention, thepatient-specific implant can be directly placed in its final and correctposition onto the bone avoiding the risk of inaccurate re-insertionafter pre-drilling or other preparatory operations, which is often aproblem when using customized bone guides. Accordingly, the customizedguides according to the present invention allow for a much more correctand accurate fixation of the implant onto the bone in comparison withthe known surgical guides used in bone and/or (complex) jointarthroplasty.

In a first aspect, the present invention provides customized surgicalguides for patient-specific bone implants, more particularly boneimplants having a patient-specific morphology, most particularly boneprostheses.

In particular embodiments, the customized surgical guides for surgicalinstruments for placement on a patient-specific implant according to theinvention comprise (i) one or more customized surface structuresextending over at least part of the patient-specific morphology of theimplant, and/or (ii) one or more customized guiding elements, and arecharacterized in that the guide and the bone implant engage by means ofa unique fit, ensured by the complementarity between saidpatient-specific morphology of said bone implant and at least one ofsaid one or more customized surface structures and/or a unique fitensured by the complementarity between said bone implant and one or morecustomized guiding elements. Additionally or alternatively thecustomized surgical guides for surgical instruments for placement on apatient-specific implant according to the invention comprise one or morecustomized locking features, and are characterized in that the guide andthe bone implant engage by means of a unique fit, ensured by thecomplementarity between said morphology of said bone implant and atleast one of said one or more of said locking elements.

More particularly, provided herein is a customized surgical guide forguiding surgical instruments for placement on a patient-specific boneimplant, said customized surgical guide comprising:

one or more customized guiding elements; and

at least one locking feature;

wherein said customized surgical guide and said bone implant engage bymeans of a unique fit, ensured by the position and orientation of saidlocking feature.

In particular embodiments, the customized surgical guides according tothe present invention are specifically suitable for placement on a boneimplant having a patient-specific morphology, i.e. a shape which isspecific for each patient and comprise (i) one or more customizedsurface structures extending over at least part of the patient-specificmorphology of the implant, and (ii) one or more customized guidingelements and are characterized in that the customized surgical guide andthe patient-specific bone implant engage by means of a unique fit,ensured by the complementarity or congruency between saidpatient-specific morphology and at least one of said one or morecustomized surface structures. In the latter embodiments, the unique fitis optionally further ensured, by the position and orientation of thecustomized guiding elements. In particular embodiments, the customizedsurgical guides further comprise one or more customized locking featuresand the unique fit is further ensured by the position and orientation ofthe customized locking features.

In particular embodiments, the one or more customized surface structuresof the surgical guides of the invention extend along thepatient-specific surface of the implant in at least two, moreparticularly at least three different main directions, to further ensurethe stability of the guides.

In particular embodiments, the customized surgical guides forpatient-specific bone implants, and more particularly the customizedsurface structures thereof are made by additive manufacturing.

In particular embodiments, the customized surgical guides of theinvention may further comprise one or more connecting structures,interconnecting the one or more surface structures and the one or moreguiding elements. In these specific embodiments, the one or more guidingelements may be attached to the one or more connecting structures.

In further particular embodiments, the one or more surface structuresand/or the one or more guiding elements and/or the connecting structureof the customized surgical guides of the invention may comprise one ormore locking features, which can be integrated in the surface structuresor connecting structure and/or which may be extensions of the one ormore guiding elements. These one or more locking features serve to lockthe surgical guide to the patient-specific implant in a certain fixedposition. In certain embodiments, a locking feature as envisaged hereinforms an extension of one of said guiding elements. In furtherembodiments, said locking feature fits into a screw hole of saidimplant.

In particular embodiments, the surgical guides according to theinvention do not comprise a dedicated locking feature.

In certain embodiments, the one or more guiding elements of thecustomized surgical guides of the invention are drill guiding elementsor cutting guiding elements. In further particular embodiments, theguiding elements further comprise a stop, such as a drill stop or acutting stop.

In particular embodiments, the customized surgical guides according tothe present invention further comprise an element, such as for example awing element, serving as a visual reference.

In particular embodiments, the customized surgical guides are designedto fit on a patient-specific acetabular implant. In a further particularembodiment of such guides for a patient-specific acetabular implant, theconnecting structure is a ring structure, fitting on the acetabular rimof an acetabular implant and the at least one or more surface structuresare designed to fit on one or more surfaces of the patient-specificacetabular implant. More particularly, the customized surgical guide andthe acetabular implant engage in a unique fit ensured by the congruency,more particularly the complementarity between the patient-specific(external) morphology of the acetabular implant and at least one of saidone or more customized surface structures and/or the orientation andposition of the locking features and/or guiding elements. In particularembodiments the unique fit ensured by the congruency or complementaritybetween the patient-specific (external) morphology of the acetabularimplant and at least one of the one or more customized surfacestructures, fitting on the surface of the patient-specific acetabularimplant. Such surfaces of the patient-specific acetabular implantoptionally include surfaces which are designed for positioning on theischium, ilium and/or the pubis and optionally ensure replacement of oneor more parts thereof. Indeed, in particular embodiments the implant isdesigned based on information obtained from patient-specific medicalimages of the ischium, ilium and/or the pubis and uniquely matches withthe specific bone geometry of the ischium, ilium and/or the pubis of thepatient in which it is introduced resulting in a patient-specificmorphology of the implant. In a particular embodiment, one surface isprovided which is designed for positioning on the ilium.

In yet a further aspect, the present invention provides methods formanufacturing customized surgical guides for a patient-specific boneimplant according to the invention. In particular embodiments, themethods of the present invention comprise a manufacturing process whichensures that the guiding elements are positioned corresponding topre-determined screw insertions, and one or more surface structures ofthe guide fit specifically on the patient-specific bone implant.

In particular embodiments, the methods comprise the steps of: (a)obtaining an image of the bone and the design of the patient-specificimplant thereon; (b) determining one or more screw trajectories using aplanning; (c) designing a customized surgical guide such that theguiding elements are positioned corresponding to the pre-determinedscrew trajectories. The methods as envisaged herein further encompassdesigning the customized surgical guide such that it ensures a specificfit with the patient-specific implant. This can be ensured in differentways. In particular embodiments, the methods comprise designing thecustomized surgical guide such that one or more surface structuresprovide a supportive structure connecting the one or more guidingelements and fit specifically on the patient-specific bone implant;additionally or alternatively, the methods comprise designing thecustomized surgical guide such that one or more locking features on thesurgical guide ensure that the surgical guide can be fixed to thepatient-specific implant in a predetermined position.Typically, the methods further comprise the step of (d) manufacturingthe customized surgical guide based on the information provided in step(c).

In further particular embodiments, the methods for manufacturing acustomized surgical guide for surgical instruments for placement on apatient-specific bone implant according to the invention, comprise thesteps of: (a) designing a customized surgical guide comprising one ormore custom guiding elements and optionally one or more locking featuresand/or one or more customized surface structures based on: (i) an imageof the bone and the patient-specific bone implant thereon and (ii) theone or more screw trajectories determined by pre-operative planning; Themethods further comprise step (b) of producing, preferably by anadditive manufacturing technique, the customized surgical guide based onthe design obtained in step (a), wherein: the one or more guidingelements of said guide are positioned corresponding to thepre-operatively planned screw trajectories, and the one or morecustomized surface structures of the guide ensure a unique fit betweenthe patient-specific bone implant and the guide by way of thecongruency, more particularly the complementarity between the customizedsurface structure and the patient-specific morphology of thepatient-specific bone implant and/or the one or more locking featuresensuring a unique fit between the patient-specific bone implant and saidguide in a predetermined position. In particular embodiments the methodcomprises ensuring that said one or more locking features fit into oneor more screw holes in said implant. In further embodiments, said one ormore locking features form an extension of said one or more guidingelements.

In particular embodiments of the methods of the present invention it isenvisaged that the one or more guiding elements of the guides arepositioned to correspond to one or more screw trajectories which havebeen determined through pre-operative planning. According to particularembodiments, the methods comprise the step of determining one or morescrew insertions using a planning taking into account one or more of thefollowing criteria:

-   -   obtaining an optimal number of non-intersecting drill directions        for screw trajectories    -   ensuring that the screw trajectories run through bone volume        with the optimal available quality    -   ensuring optimal screw trajectory length and    -   ensuring that the surrounding healthy soft tissue is optimally        preserved.        In particular embodiments the step of ensuring that the screw        trajectories run through bone volume with the optimal available        quality is determined from grey values in medical images.

The customized surgical guides obtainable by the methods according tothe present invention not only ensure an improved accuracy compared toprior art guiding tools, but in addition make it possible to provideguidance in complex bone reconstructions. Thus, surgical guidesobtainable by the methods of the present invention are novel andinventive over the standard guides or even the alleged “custom” guidesdisclosed in the prior art.

In a further aspect, the present invention provides combinations of apatient-specific bone implants, and a customized surgical guideaccording to the invention. It will be understood that the customizedsurgical guides according to the invention are designed to fitspecifically onto the patient-specific bone implant of the combination.

More particularly, provided herein is a combination of apatient-specific bone implant and a customized surgical guide forsurgical instruments for placement on said patient-specific boneimplant, said customized surgical guide comprising one or morecustomized guiding elements and one or more elements which ensure aunique fit between said customized surgical guide and said implant. Inparticular embodiments, said customized surgical guide comprises one ormore customized surface structures and/or at least one locking feature,wherein said customized surgical guide and said bone implant engage bymeans of a unique fit, ensured by the position and orientation of saidone or more customized surface structures and/or said at least onelocking feature.

In a further aspect, the present invention relates to the use of theguides according to the invention for fixing a patient-specific boneimplant onto a bone. More particularly, the invention provides methodsfor fixing a patient-specific bone implant onto a bone, comprising thesteps of: (a) placing a customized surgical guide according to theinvention onto a patient-specific bone implant; (b) introducing thescrew trajectories with the appropriate surgical tools; (c) removing thecustomized surgical guide; and (d) fixing the patient-specific boneimplant with screws onto the bone, whereby step (d) of fixing thepatient-specific implant can be either prior to or after step (c), orboth. More particularly said method may comprise in step (a) ensuringthe correct positioning of said customized surgical guide onto saidpatient-specific bone implant by positioning said one or more customizedsurface structures of said customized surgical guide on saidcorresponding surface(s) of said implant and/or ensuring that said atleast one locking feature of said customized surgical guide fits ontosaid implant.

The invention further provides computer programs for performing themethods of the present invention, more particularly, computer programproducts for enabling a computer to execute all or part of the methodsaccording to the invention described herein. More particularly, computerprograms are provided for providing a design of a customized surgicalguide comprising one or more custom guiding elements and one or morecustomized surface structures based on (1) one or more images of thebone and the patient-specific bone implant thereon; and (2) one or morescrew trajectories determined by pre-operative planning, wherein the oneor more guiding elements of the guide are positioned corresponding tothe pre-operatively planned screw trajectories, and the lockingfeature(s) and/or one or more customized surface structures of the guideensure a unique fit between the patient-specific bone implant and theguide by way of a congruency or complementarity between the lockingfeature(s) and/or said customized surface structure(s) and thepatient-specific morphology of the patient-specific bone implant.

BRIEF DESCRIPTION OF THE DRAWINGS

The following description of the figures of specific embodiments of theinvention is merely exemplary in nature and is not intended to limit thepresent teachings, their application or uses. Throughout the drawings,corresponding reference numerals indicate like or corresponding partsand features.

FIG. 1 Example picture of a customized surgical drill guide for apatient-specific acetabular implant according to a particular embodimentof the present invention.

FIG. 2A Drawing of a left hemi-pelvis with a large acetabular bonedefect

FIG. 2B Drawing of a left hemi-pelvis with a large acetabular bonedefect reconstructed by a patient-specific acetabular implant.

FIG. 2C Complete assembly of a left hemi-pelvis with a large acetabularbone defect with a patient-specific implant and a customized surgicalguide according to a particular embodiment of the invention.

FIG. 2D Zoomed view on the central portion of a customized surgicalguide according to a particular embodiment of the invention.

FIG. 2E Zoomed view on cylindrical drill guiding elements of acustomized surgical guide according to a particular embodiment of theinvention, wherein the guiding elements are positioned on thepatient-specific ilium area of the implant.

FIG. 3 A customized surgical guide according to a particular embodimentof the invention designed to fit on a patient-specific acetabularimplant.

FIG. 4 Cross-sectional view of a cylindrical drill guiding element of acustomized surgical guide according to a particular embodiment of theinvention, with (right) and without (left) extension.

FIG. 5 A customized surgical guide according to a particular embodimentof the invention comprising a wing element serving as a visual referencefor performing a surgical interaction.

FIG. 6 A customized surgical guide according to a particular embodimentof the invention comprising a cylindrical drill guiding element that ishalved lengthwise, allowing for instance (partial) insertion of a screwdirectly in the implant, and subsequent removal of the customized guidewith the inserted screw left in place.

FIG. 7 Illustration of a right hemi-pelvis with an acetabular bonedefect reconstructed by a patient-specific acetabular implant accordingto an embodiment envisaged herein.

FIG. 8 Front view (A) and rear view (B) of a particular embodiment ofthe customized surgical guide described herein, designed to fit on apatient-specific acetabular implant.

FIG. 9 Complete assembly of a hemi-pelvis with an acetabular bone defectwith a patient-specific implant and a particular embodiment of thecustomized surgical guide described herein.

FIG. 10 Side view of an assembly of a patient-specific acetabularimplant and a particular embodiment of the customized surgical guidedescribed herein.

FIG. 11 Top view (A) and perspective view (B) of a complete assembly ofa hemi-pelvis with an acetabular bone defect with a patient-specificimplant and a particular embodiment of the customized surgical guidedescribed herein.

FIG. 12 Illustration of a particular embodiment of the customizedsurgical guide described herein.

FIG. 13 Illustration of a patient-specific acetabular implant.

List of reference numerals used in the Figures. Each of theseillustrations represent particular embodiments of the features concernedand the corresponding features are not to be interpreted as limited tothis specific embodiment.

-   (1) Bone model: left hemi-pelvis-   (2) Patient-specific acetabular implant-   (3) Customized surgical guide according to a specific embodiment of    the invention-   (4) Drill directions or screw trajectories-   (5) Central (interconnecting) ring structure, designed to fit    specifically with the acetabular rim of the patient-specific implant    according to a specific embodiment of the invention-   (6) Locking features (an example, e.g. on central ring Structure    (5))-   (7), (8) and (9) One or more surface structures-   (10) and (11) One or more guiding elements-   (12) Implant screw holes-   (13) Acetabular rim of the patient-specific implant-   (14) Cavity formed by the acetabular portion of the patient-specific    implant-   (15) Ends of cylindrical guiding elements, which are trimmed either    straight, obliquely or with a complexly shaped cut-   (16) Extension of cylindrical guiding elements-   (17), (18) and (19) Patient-specific areas on external surface of an    acetabular implant-   (20) Disc-shaped visual reference ring-   (21) Bridging element-   (22) Wing element serving as a visual reference for performing a    surgical interaction-   (23) Cylindrical guiding elements that are halved lengthwise-   (24) Bone model: right hemi-pelvis-   (25) Patient-specific acetabular implant-   (26) Customized surgical guide according to a specific embodiment of    the invention-   (27) Drill cylinder (28) Surface structure-   (29) Patient-specific contact surface of acetabular implant-   (30) Patient-specific acetabular implant-   (31) Customized surgical guide according to a specific embodiment of    the invention-   (32) Locking feature

DETAILED DESCRIPTION

The present invention will be described with respect to particularembodiments but the invention is not limited thereto but only by theclaims. Any reference signs in the claims shall not be construed aslimiting the scope.

Where the term “comprising” is used in the present description andclaims, it does not exclude other elements or steps. Where an indefiniteor definite article is used when referring to a singular noun e.g. “a”or “an”, “the”, this includes a plural of that noun unless somethingelse is specifically stated.

Furthermore, the terms first, second, third and the like in thedescription and in the claims, are used for distinguishing betweensimilar elements and not necessarily for describing a sequential orchronological order, unless specified. It is to be understood that theterms so used are interchangeable under appropriate circumstances andthat the embodiments of the invention described herein are capable ofoperation in other sequences than described or illustrated herein.

The terms or definitions used herein are provided solely to aid in theunderstanding of the invention.

The present invention provides customized surgical guides forpatient-specific bone (or joint) implants, which allow both a stableintroduction of a surgical instrument into a bone (or a joint) as wellas ensuring an accurate fixation of the implant onto the bone (orjoint).

The term patient-specific implant as used herein refers to an implant ofwhich at least part is shaped to match the specific bone geometry of apatient. Thus, a guide according to the present invention is envisionedto fit specifically onto an implant which itself is specific for aparticular patient. In the context of the present invention, and moreparticularly when referring to the unique fit of the guide on thepatient-specific implant, the terms “congruency” and “complementarity”are used. It is considered that two surfaces are “congruent”, when thesurface features match, which can be as a result of a similarity offeatures (one surface corresponding essentially to a mold taken from theother) and/or as a result of the fact that one or more specific featuresof one surface are designed to fit onto the other surface. The term“complementary” more strongly emphasizes the similarity of the features.In the context of a patient-specific implant this typically implies thatthe one or more contact surface(s) of the implant are complementary tothe remaining area(s) of the bone or joint, and thereby ensure a(patient)-specific fit. This specific fit of the implant is ensuredduring the planning and design of the implant, and may imply that inspecific areas a clearance of between 0.1 and 0.5 mm between the implantCAD model and the prepared bone CAD model is envisaged. In the contextof the guides of the present invention, this implies that the one ormore contact surface(s), locking features and/or guiding elements of theguide are complementary to the external surface of the implant, suchthat they ensure a (patient- and implant-) specific fit.

In particular embodiments of the present invention, the patient-specificimplants are replacement bone prostheses, i.e. they replace at leastpart of a bone or joint lost by injury (traumatic) or missing from birth(congenital). This type of replacement bone prosthesis is different frommedical devices such as screws or plates which merely serve to secureexisting bone parts to each other. These patient-specific implants, inaddition to comprising a surface which is complementary to the remainingarea(s) of the bone or joint on which the implant is to be fitted,moreover mimic and/or functionally replace the surface of the original(i.e. non-injured) and absent piece of the bone or joint. Preferably,where possible, the surface of these implants seamlessly connects to theremaining surfaces of bone adjoining the implant site. Thus, inparticular embodiments, the patient-specific implants according to thepresent invention are characterized by an “external” morphology which ispatient-specific. The “external” morphology comprises one or moresurfaces of the implant which replaces the original surface of the boneor joint. In these embodiments the implant is not only designed to fitspecifically onto remaining areas of the bone or joint to ensure aseamless restoration of the injured bone or joint, but additionally, inview of the fact that the implant at least partially replaces one ormore anatomical features of the bone or joint, mimics and/orfunctionally replaces the original anatomical features of the bone orjoint.

In certain embodiments, the outer structure or external morphology ofthe implant may be provided with a porous osteoconductive construct, topromote tissue infiltration and attachment of the implant to the bone.In further embodiments, the porous osteoconductive construct maycomprise a porous metal, such as porous tantalum. Such metals canclosely resemble the physical and mechanical properties of bone and maytherefore enable rapid and extensive tissue infiltration and strongattachment. An example of such porous metal is Trabecular Metal™(available from Zimmer).

Patient-specific implants have the advantage that they have a betteranatomic fit compared to conventional standard implants. This reducesoperating time and results in a longer-lasting and better functioningimplant. Moreover, in specific cases of reconstructive bone and jointsurgery, for example cases with large bone defects and/or malformations,patient-specific implants are simply the only alternative asoff-the-shelf implants are just unable to provide stable support andfixation, and functioning. Patient-specific implants are typicallydesigned based on medical images (such as a Computed Tomography (CT)data set) of the bone. A patient-specific implant may include anoff-the-shelf implant which is adjusted (e.g. pre-bent) to the shape ofthe bone (and/or bone defect) of the patient prior to the start ofsurgery. Patient-specific implants preferably have not only a single fit(i.e. only one position fits), but also a unique fit with the bonestructure in which they are introduced (i.e. fitting only on thespecific patient). In addition, optimally, as detailed above,patient-specific implants may have a patient-specific externalmorphology. This unique fit corresponds to the position of the surgicalguide on the implant envisioned in the planning of the surgicalintervention.

More particularly, in particular embodiments the present inventionprovides customized surgical guides for surgical instruments suitablefor placement on patient-specific bone implants, which are positionedonto the patient-specific bone implant (and not or not exclusively ontothe bone), by specifically fitting onto one or more surfaces of thepatient-specific implant. At the same time, the customized surgicalguides according to the invention establish absolute directions and/orlocations of drill and/or cut trajectories since the patient-specificimplant fits specifically onto the bone, and the guide fits uniquely(i.e. only in that position) onto the patient-specific implant.

The unique fit between the customized surgical guides and thepatient-specific implant can be ensured in one or more of the followingways.

The customized surgical guides of the present invention comprise atleast one or more surface structures and one or more guiding elements.In particular embodiments, at least one of the one or more surfacestructures is designed to fit specifically onto the external morphologyof the patient-specific bone implant. Additionally or alternatively, thecustomized surgical guides as envisaged herein comprise at least onelocking feature designed to ensure a unique tight fit with the externalmorphology of the patient-specific bone implant.

The different components of the surgical guides according to the presentinvention are described more in detail hereafter.

The customized surgical guides according to the present invention maycomprise one or more surface structures which are structures whichextend over at least part of the surface of the implant. The surfacestructures may extend over one or more generic parts of the surfaceand/or one or more patient-specific parts of the surface. The one ormore surface structures may have one or both of the following functions.In particular embodiments, the one or more surface structures ensure theunique fit of the surgical guides with the patient-specific implant.Accordingly, the surface structures comprise one or more areas by whichthe correct placement of the guide on a patient-specific implant isensured. In particular embodiments, such surface structures coincidewith and follow (i.e. are congruent or complementary to) the outerstructure (or external morphology) of the implant.

The one or more surface structures of the customized surgical guidesaccording to the present invention may also serve as a base orsupportive structure for the one or more guiding elements of the guides.

In particular embodiments, the outer structure or external morphology(i.e. the structure on the side of the implant which does not contactthe bone in which the implant is fit) of the patient-specific implant ispatient-specific. In particular embodiments, the customized guide isdesigned to fit uniquely (i.e. only in one position) onto the outerstructure of the patient-specific implant.

In particular embodiments, one or more of the surface structures of thecustomized surgical guides of the invention comprises, on the sidedesigned to fit onto the surface of the implant, at least an area(hereinafter also referred to as an ‘implant-specific area’) which isexactly and fully complementary, i.e. specifically fits onto a specificarea of the patient-specific bone implant, on which the guide is to beplaced.

In particular embodiments, the congruency or complementarity between thearea on the patient-specific implant and the area on at least one of thesurface structures of a customized guide according to the invention mayinvolve a clearance between the guide surface and the bone implant. Inparticular embodiments, this specific fit involves planning a clearanceof between 0.1-0.5 mm in the implant-specific area(s) between the guideand the implant.

In these specific embodiments of the invention, (i.e. wherein one ormore of the surface structures comprises an implant-specific area) whenone or more implant-specific areas of the one or more surface structuresare contacted with or positioned opposite to their correspondingcomplementary surfaces of the patient-specific bone implant, thesurfaces fit, mate and/or engage, thereby fixing the guide into apredetermined position. This position is not only the single position inwhich the surgical guide can be placed on the implant, but is also“unique” to the patient-specific implant (i.e. the guide will not fitwith the same accuracy on another implant). Accordingly, in theseembodiments, a unique fit between the guide and the implant is ensuredby the one or more surface structures, more particularly by theimplant-specific areas thereon.

It is noted that the customized guides according to these embodiments ofthe invention, while intended to fit uniquely onto a patient-specificimplant, may, in addition to the surfaces or parts thereof which ensurethe unique fit with the patient-specific implant, comprise surfaces orparts thereof which, upon placement, contact the bone and are supportedby the bone. Optionally, the one or more surfaces or parts thereofcontacting the bone, may comprise areas which specifically mate withareas of the bone.

In specific embodiments, the three-dimensional fit of the contact areabetween the one or more surface structures of the custom surgical guideand the patient-specific implant ensures the stability of guidepositioned onto the implant by preventing both translation and rotation(either uni- or bi-directionally) along and/or around a certain axis.

Alternatively, where the outer surface of the patient-specific boneimplant is generic, such an area of a surface structure may becustomized to fit a specific area of this generic outer surface.Moreover, the outer surface of the patient-specific implant may compriseboth patient-specific and more generic parts, such that the one or moresurfaces of the customized guides of the invention may comprise one ormore areas with a generic fit and one or more areas with apatient-specific fit.

The exact size and shape of the one or more surface structures of theguide are not critical to the invention but will be determined by theshape of the patient-specific implant. In particular embodiments thepatient-specific areas on the one or more surface structures encompassat least 30% of the surface of the guide which contacts the implant.More particularly, this extends to at least 50%, even more particularlyto between 50 and 90, or even to more than 95% of the surface of theguide contacting the implant. As detailed above, the patient-specificareas may also comprise sections which contact the bone.

In particular embodiments, the surface structures correspond to flanges,i.e. longitudinal structures which extend in one or more differentdirections and allow for exact and stable fitting of the custom guideonto the implant and/or supporting of one or more guiding elements formaking drilling or cutting trajectories from the implant into one ormore underlying bone structures. According to these embodiments,customized surgical guides with one or more, two or more, three or moreflanges are envisaged. Such flanges may be connected through one or moreconnecting structures as detailed below. In particular embodiments, theone or more customized surface structures of the surgical guides of theinvention extend along the patient-specific surface of the implant in atleast two, more particularly at least three different directions, tofurther ensure the stability of the guides. In further particularembodiments the customized guides according to the present inventioncomprise at least three flanges which, projected onto a plane extendinto three directions on the surface (in the plane of the surface) ofthe implant of which at least two directions are separated less than180° C.

However, it is envisaged that in certain embodiments, the guidinginstrument does not comprise one or more flanges as described above.Indeed, bone implants for the repair of small bone defects often provideonly a relatively small external surface, such that flanges can not beused. Accordingly, in certain embodiments, the guiding instrument maycomprise a single guiding element for positioning onto apatient-specific implant. Such guiding element preferably is providedwith one or more locking features (see further).

In particular embodiments, the customized surgical guides of theinvention, irrespective of their other features, may comprise one ormore locking features, which provide an (additional) interlock of thesurgical guide with the patient-specific guide. Such interlockingfeatures may be a three-dimensional feature designed specifically on aguide/implant combination. Although the unique fit of the guide with theimplant may be ensured by the surface structures and/or guiding elementsalone, the locking features may additionally or alternatively ensurefitting and maintenance of the guide in the unique fit position. Incertain embodiments, the unique fit of the guide with the implant maythus be ensured by the locking features alone, or by a combination oflocking features and surface structures. In particular embodiments, theposition and/or orientation of the locking feature ensures a unique fitwith the implant. In particular embodiments, the locking feature is anextension which fits into a hole on the surface of the implant. Infurther embodiments, the locking feature fits into a hole correspondingto a screw trajectory on the implant.

In particular embodiments, the guides according to the invention do notcomprise a specific locking feature. In further particular embodiments,the surgical guides according to the invention do not comprise a lockingfeature positioned on a surface structure.

The customized surgical guides of the present invention further compriseone or more guiding elements for guiding a surgical instrument or toolinto the bone (or joint) of a patient. The one or more guiding elementseach contain at least one means of guiding an instrument such as but notlimited to a drill, bur, saw, jig saw, lateral drill or any othercutting, milling or drilling instrument or any other tool such as afastener, more particularly a screw, the orientation and position ofwhich corresponds to a planning.

Where the tool is a screw or the surgical instrument is a drill or bur,a guiding element of the surgical guide according to the invention maycomprise at least a cylindrical hole. Where the guide is a drill guide,the diameter of the drill guiding element is determined based on thediameter of the pre-drill instrument. In particular embodiments, wherethe surgical instrument is a saw, jig saw, mill or lateral drill, aguiding element may contain at least a (narrow) slot or flat surface.The height of the one or more guiding elements of the surgical guideaccording to the invention is determined to provide sufficient stabilityand/or guidance to the surgical instrument which is to be introduced.

The guiding element of the surgical guide according to the invention aretypically cylindrical, but the ends (15) may be trimmed either straight,obliquely or with a complexly shaped cut (see FIG. 2E), in order to fitthe available working space and/or surgical window. More specifically,the entire customized surgical guide has to fit into the typicallyV-shaped surgical incision space during application, and shouldtherefore enable (temporary) soft tissue overlay when put under—forinstance—muscles.

The one or more guiding elements can optionally include a safety stop toprevent a surgical instrument from advancing beyond a planned depth intothe bone. For example, in the case where the surgical instrument to beintroduced into the bone or joint is a drilling instrument, such as adrill or a bur, drill stops may be used to prevent the surgical drillfrom advancing beyond a planned or determined depth into the bone.Alternatively, in the case where the surgical instrument to beintroduced into the bone or joint is a cutting instrument, such as a sawor a jig saw, cutting stops may be used to prevent the surgical cuttinginstrument from advancing beyond a planned or determined depth into thebone.

The guiding elements can further be adjusted to allow fastening of theimplant prior to drilling and/or removal of the guide. For instance, acylindrical drill guiding element can be halved lengthwise (as shown inFIG. 6), allowing (partial) insertion of a screw directly in theimplant, and subsequent removal of the customized guide with theinserted screw left in place. Doing so reduces degrees of freedom of thepatient-specific implant and customized guide during drilling, andassures that correspondence between pre-drills and screw holes is notlost. For instance, where the type of screw is a self-tapping type ofscrew, pre-drilling is not required, allowing direct insertion of thescrew and immediate establishing of the screw trajectory along thepredetermined path.

The position of a guiding element comprised in the surgical guidesaccording to the present invention is typically determined by theplanned direction of a surgical instrument into the bone or joint. Assuch the guiding elements are “customized” to the specific requirementsas determined by the planning. The patient-specific implant willtypically be provided with holes corresponding to the pre-determinedscrew insertions and the position of the guiding elements in thecorresponding custom surgical guide is ensured to allow guiding of asurgical instrument through these holes.

In particular embodiments, the customized guiding elements ensure(optionally in addition to implant-specific surface structures and/orlocking features described above) a unique fit of the surgical guidewith a patient-specific implant. Indeed, it is envisaged that a uniquefit between the implant and the guide can be ensured by matching of theguiding elements on the implant according to the pre-determinedoperative planning. Accordingly, in particular embodiments, the uniquefit is ensured by the guiding elements or a combination of guidingelements, locking features and/or implant-specific surface structures.In particular embodiments, the unique fit between the implant and theguide is ensured by at least 30% of the total contact surface (i.e.including implant-specific surfaces and guiding elements) between theguide and the implant, more particularly by at least 50% of the totalcontact surface, even more particularly by at least 75% of the totalcontact surface. In particular embodiments the unique fit is ensured by95 to 100% of the total contact surface of the guiding element. However,where the unique fit is ensured by the locking features alone, this mayrepresent 5-10% of the total contact surface.

As determined by the nature of the implant, the guiding elements aretypically positioned on one or more surface structures and/or on theconnecting structure. Elements of the connecting structure which ensurethe connection of one or more guiding elements with the remainder of thesurgical guide are also referred to herein as ‘bridging elements’.

In preferred embodiments, the one or more guiding elements arepositioned either on the one or more surface structures or on the one ormore connecting structures (as further described herein) such that asurgical instrument which is passed through the one or more guidingelements can engage the bone or joint at a desired location. Theposition of the one or more guiding elements is also such that it allowsinsertion of a surgical instrument. In specific embodiments, thedirections of the one or more guiding elements are mutually intersectingin order to allow the guiding elements to all be positioned within theavailable working space and/or surgical window.

In particular embodiments, the one or more guiding elements of thecustomized surgical guides of the invention may comprise one or morelocking features, which (help to) ensure a specific and stable fit withthe patient-specific implant. In certain embodiments, the guidingelement described herein comprises two, three, four, five, six, seven,eight, or more locking features. The locking features typically fitspecifically onto the morphology of the patient-specific implant. Inparticular embodiments, one or more of the at least one locking featurecomprises an extension of the guiding element which fits into theimplant screw hole, while still allowing insertion of the surgicalinstrument, as for example shown in FIG. 4. Such extensions can also beseen in FIG. 8, which provides a front view (A) and rear view (B) of aparticular embodiment of the surgical guiding instrument (26) describedherein, designed for positioning on an acetabular implant (25), as shownin FIGS. 7, 9 and 10. In particular embodiments, the guiding instrumentis provided externally with a plurality of locking features, wherein thesize and position of the locking features correspond to the size andposition of a plurality of screw holes provided on the acetabularimplant. In these embodiments, the locking feature typically correspondsto a three-dimensional extension of the guiding element. Such anextension may be cylindrical or may have an angular cross-section.

The locking feature(s) may also fit onto structures of the implant otherthan screw holes. Indeed, the locking features may fit onto any featureof the implant which allows for obtaining a stable and unique fit. Forexample, one or more locking features may be designed to laterallyengage with one or more features on the implant, such that a unique andstable fit is ensured. In particular embodiments, the locking featuresmay engage a feature on one or more flanges of an implant containingpatient-specific surfaces. In particular embodiments, the guidingelement may comprise two locking features which simultaneously engagewith two features (e.g. protrusions) on the implant, whereby therelative position of said features ensures a tight lock of said lockingfeatures restricting rotational movement of the guide with respect tothe implant. In particular embodiments, the implant comprises dedicatedfeatures for receiving the locking feature of the guide. Accordingly, aunique and stable fit of the guiding instrument on the implant can beachieved by positioning the locking features of the guiding instrumentonto the implant. Indeed, a locking feature can ensure a unique fit(i.e. fitting only in one position relative to each other) between theguiding instrument and the implant as a result of its specific positionand orientation on the guide.

In further particular embodiments, the guides of the present inventiondo not comprise a specific (i.e. independent) locking feature. Infurther particular embodiments, the surgical guides of the invention donot comprise a dedicated locking feature positioned on a guidingelement.

As mentioned above, according to specific embodiments, the surgicalguides of the present invention may further comprise one or moreconnecting structures, which directly or indirectly connect the one ormore surface structures to the one or more guiding elements in thecustomized surgical guides according to the invention. In certainembodiments, the connecting structures directly or indirectly connectthe one or more guiding elements to each other and/or to the lockingfeature(s).

The one or more connecting structures of the surgical guides accordingto the present invention must be sufficiently rigid, so as to ensure thedesired stability and accuracy upon use of the guide, and shouldnevertheless be as open as possible, so as to allow visual verificationfor the surgeon of the good fit of the surgical guide. Accordingly, inparticular embodiments, the one or more connecting structures of thesurgical guides according to the present invention ensure a mechanicallyrigid but (from a utilitarian point of view) versatile connectionbetween the one or more surface structures and the one or more guidingelements in the customized surgical guides, such that the position ofthe different components of the guide relative to each other is fixed.

Similar to the surface structures described above, the one or moreconnecting structures comprised in the customized surgical guideaccording to the invention may have one or more of the followingfunctions. In addition to serving to interconnect the one or moresurface structures and the one or more guiding elements, the one or moreconnecting structures may serve as a base or supportive structure forone or more guiding elements. Additionally or alternatively, the one ormore connecting structures may help to ensure a specific fit with thepatient-specific implant.

As will be detailed below, where the customized surgical guide accordingto the invention is a customized guide for a patient-specific acetabularimplant, the one or more connecting structures can comprise a ringstructure designed to fit specifically with the acetabular rim of thepatient-specific implant. The one or more connecting structures mayfurther comprise bridging structures, which ensure the connection of oneor more guiding elements for guiding surgical tools into the acetabularcup with the remainder of the surgical guide.

In further particular embodiments, the one or more connecting structuresof the customized surgical guides of the invention may comprise one ormore locking features, which ensure an (additional) interlock with thepatient-specific implant. Where the one or more connecting structurescomprise a circular ring designed to fit on an acetabular rim of anacetabular implant, such locking features can be positioned on the ringstructure to ensure an interlock with the acetabular rim of thepatient-specific implant. As detailed above, however, in particularembodiments, the surgical guides of the present invention do notcomprise a locking feature, more particularly do not comprise a lockingfeature positioned on the connecting structure.

The customized surgical guiding tools of the present invention mayfurther comprise one or more features for visual referencing, to solveorientation problems in case of complexly shaped guiding elements. Thesevisual references may optionally be attached to the surgical guides toprovide a (visual) feedback to the surgeon, more particularly in case ofdrill guiding elements with overlying soft tissue, minimizing potentialmisinterpretation resulting from obscured anatomical reference points,or potentially confusing orientations of the surface structures of thecustomized guide. Such visual reference may for example include areference disc (20), as shown in FIGS. 2E and 4, whereby the planeformed by the disc is perpendicular to the planned drill direction.Additionally or alternatively, the customized guide according to thepresent invention may further comprise one or more elements, such aswing elements (22), exemplified in FIG. 5, or planar discs, indicatingthe direction and/or position of the one or more drill guiding elementsof the guide and thus also serving as a visual reference. Such visualreferences can be attached to a drill guiding element or any otherportion of the customized guide.

In a further aspect, the present invention provides combinations of apatient-specific bone implant and a customized surgical guide accordingto the invention (as described above). Indeed, it is the object of thepresent invention to provide a customized surgical guide which fitsspecifically onto a patient-specific bone implant. Accordingly, as thesurgical guide is designed to fit specifically on the bone implant, itis envisaged that the implant and guide are provided in combination. Inspecific embodiments of combinations of a patient-specific bone implantand a customized surgical guide according to the invention (i.e. whereinone or more of the surface structures comprises an implant-specificarea) when one or more implant-specific areas of the one or more surfacestructures are contacted with or positioned opposite to theircorresponding complementary surfaces of the patient-specific boneimplant, the surfaces fit, mate and/or engage, thereby fixing the guideinto a predetermined position. This position is unique to thepatient-specific implant, and since the patient-specific implant in turnhas a unique position to the bone, the customized guide has a uniqueposition to the bone.

Additionally or alternatively in the envisaged combinations, thecustomized surgical guide and the bone implant engage by means of aunique fit ensured by the position and/or orientation of the one or morelocking features. This unique fit ensures that the guide can be fixedinto a predetermined position

The customized surgical guides according to the invention are envisagedfor use with different types of bone implants. The surgical guides ofthe present invention are of particular interest for use in the fixationof bone implants in the context of complex bone reconstructions, i.e.where bone loss is observed. Thus, the guides of the present inventionare particularly suited for implants which replace deficient or missingbone structures. The surgical guides of the present invention are alsoof particular use where a limited surgical window is/can be used.However, the customized surgical guides according to the presentinvention can be designed for any patient-specific implant. The use ofpatient-specific implants has a number of advantages compared totraditional off-the shelf implants. They ensure a better and tighteranatomic fit which results in a better stability and/or function (lessaseptic loosening) and reduced damage to neighboring tissue. The timerequired by the surgeon for placement (operating time) is reduced.Moreover, for particular applications (such as in Cranio-Maxillo-Facialsurgery) patient-specific implants ensure a more satisfying aestheticresult for the patient. Patient-specific implants are commonly used inorthopedic surgery of the knee, hip and shoulder, but the customizedsurgical guides according to the invention are equally suitable for usein combination with patient-specific implants for other joints or bones.Accordingly, the combinations according to the present invention are notlimited by a specific type of patient-specific implant.

In particular embodiments, the combination of a customized surgicalguide and a patient-specific implant according to the invention is acombination of a patient-specific acetabular implant and a customizedsurgical guide therefore. As detailed above, the customized surgicalguide for an acetabular implant may comprise one or more connectingstructures comprising a ring structure and one or more surfacestructures of the guide are designed to fit on one or more surfaces ofthe patient-specific acetabular implant. In certain embodiments, apatient-specific acetabular implant comprises one or more extensionsdesigned for positioning on one or more of the ischium, ilium and/or thepubis. In particular embodiments, the corresponding customized surgicalguide comprises one or more surface areas which are designed to fit ontothe one or more extensions of the implant. In a further particularembodiment the customized surgical guide comprises one surface structuredesigned to fit onto an extension of a patient-specific implant whichfits onto the ilium. However, it is envisaged that in certainembodiments, the implant does not comprise extensions as mentioned abovesuch that the customized surgical guide does not require correspondingextensions.

The combinations according to the invention comprise, in addition to apatient-specific implant, a customized surgical guide thereforeaccording to the invention. Accordingly, the customized surgical guidecomprises one or more guiding elements and one or more surfacestructures and/or at least one locking feature to ensure a unique fitbetween said implant and said customized surgical guide. Optionally, andas described in detail above, the customized surgical guide for use in acombination with the corresponding patient-specific implant comprisesone or more connecting structures interconnecting the one or guidingelements with the one or more surface structures and/or the one or morelocking features.

In particular embodiments of the combinations comprising apatient-specific bone implant and a customized surgical guide accordingto the invention, the one or more surface structures and/or the one ormore guiding elements and/or the connecting structure of the customizedsurgical guides may comprise one or more locking features, which can beintegrated in the surface structures or connecting structure and/orwhich may be extensions of the one or more guiding elements and whichensure (additional) specific interlock with the patient-specificimplant.

In further particular embodiments of the combinations according to theinvention, the one or more guiding elements of the customized surgicalguides are drill guiding elements (or even cutting guiding elements). Infurther particular embodiments, the guiding elements further comprise astop, such as a drill stop.

Particular embodiments of the combinations of the present inventioncomprise a patient-specific implant and two or more customized surgicalguides.

As detailed above, the customized surgical guides and the combinationsthereof with patient-specific implants according to the presentinvention are suitable for use in any type of bone or joint surgeryprocedure, such as for example bone or joint replacement surgery and/orbone or joint reconstruction surgery. Some non-limiting examples ofjoints in which patient-specific implants may be used and thus in whichthe customized surgical guides and the combinations thereof withpatient-specific implants according to the present invention can beapplied include the hip joint (or acetabulofemoral joint) between thefemur and acetabulum of the pelvis, the shoulder joints (such as theglenohumeral joint between the humerus and the lateral scapula), thewrist joint (or radiocarpal joint) between the radius and the carpus,the elbow joints (such as the humeroulnar joint between the ulna and thehumerus), the knee joints (the femoropatellar articulation between thepatella and the femur or the femorotibial articulations between thefemur and the tibia), and the ankle joint (or talocrural joint) betweenthe tibia and fibula. Non-limiting examples of bone surgery proceduresin which the customized surgical guides and the combinations thereofwith patient-specific implants according to the present invention can beapplied include intercalar resections, plating (osteosynthesis),epiphysis of long bones, diaphysis of long bones, treatment ofcomminuted fractures, and arthrodesis.

Accordingly, the customized surgical guides and the combinations thereofwith patient-specific implants according to the present invention can beused in any type of bone or joint surgery procedure for the treatment ofa variety of bone and/or joint diseases, including but not limited toosteoarthritis, rheumatoid arthritis, avascular necrosis, osteonecrosis,congenital disease, dislocation of a joint, joint dysplasia, frozenshoulder, loose shoulder, traumatized and maligned joint, and jointstiffness. In particular embodiments, the surgical guides andcombinations thereof with patient-specific implants are used in thetreatment of acetabular bone deficiencies. More particularly, the guidesare of interest for use in acetabular defects which are optimallytreated with patient-specific implants, such as those classified as type3 or 4 deficiencies according to the AAOS classification (D'Antionio etal. 1999, Clin Orthop Rel Res, 243:126-137)) or as type IIIb accordingto the Paprosky classification (Paprosky et al. 1994, J Arthroplasty9(1):33-44).

In a further aspect, the present invention provides methods formanufacturing customized surgical guides for patient-specific boneimplants.

In particular embodiments, the methods for manufacturing a customizedsurgical guide for surgical instruments for placement on apatient-specific bone implant according to the invention comprise thesteps of generating, a customized surgical guide wherein the one or moreguiding elements of the guide are positioned corresponding to thepre-operatively planned screw trajectories and/or the one or morecustomized surface structures and/or locking features of the guideensure a unique fit between the patient-specific bone implant and saidguide. In particular embodiments said unique fit is ensured by way ofthe congruency and/or complementarity between said customized surfacestructure and the external morphology of said patient-specific boneimplant. In particular embodiments, the locking feature(s) ensure aunique fit between the bone implant and the guide by the position and/ororientation of the locking feature on the guide. In particularembodiments, said locking feature(s) interlock with screw hole(s) on theimplant. In further particular embodiments, the guide is made by anadditive manufacturing technique based on a design generated based onpre-operative planning. Thus in particular embodiments, the methods ofthe invention comprise:

(a) designing a customized surgical guide comprising one or more customguiding elements and one or more customized surface structures based on:

an image of the bone and the patient-specific bone implant thereon;

the one or more screw insertions determined by pre-operative planning

(b) producing, preferably by an additive manufacturing technique, saidcustomized surgical guide based on the design obtained in step (a),wherein:

the one or more guiding elements of said guide are positionedcorresponding to the pre-operatively planned screw trajectories, and

the one or more customized surface structures of said guide ensure aunique fit between the patient-specific bone implant and said guide byway of the congruency between said customized surface structure and thepatient-specific morphology of said patient-specific bone implant and/or

the one or more locking features ensure a unique fit between thepatient-specific bone implant and said guide. In particular embodiments,the methods for manufacturing customized surgical guides according tothe invention comprise the steps of:

(a) obtaining an image of the bone and the patient-specific implantthereon;(b) determining one or more screw insertions using a planning;(c) designing a customized surgical guide such that

-   -   the guiding elements are positioned corresponding to the        pre-determined screw trajectories, and    -   the one or more locking features fit uniquely onto the        patient-specific implant; and/or one or more surface structures        provide a supportive structure connecting the one or more        guiding elements and fit uniquely on the patient-specific bone        implant.        (d) producing said customized surgical guide based on the        information provided in step (c).

Accordingly, the methods of manufacturing of the customized surgicalguides according to the invention comprise the step of obtaining animage of the bone and the patient-specific implant thereon. Digitalpatient-specific image information can be provided by any suitable meansknown in the art, such as for example a computer tomography (CT)scanner, a magnetic resonance imaging (MRI) scanner, an ultrasoundscanner, or a combination of Roentgenograms. A summary of medicalimaging has been described in “Fundamentals of Medical imaging”, by P.Suetens, Cambridge University Press, 2002.

For example, the step of obtaining an image of the bone and thepatient-specific implant thereon may for example comprise the steps of(a1) obtaining 2D datasets of the bone and (a2) reconstructing a 3Dvirtual bone model from said 2D datasets. Indeed, the first step in aplanning is the construction of a 3D virtual model of the bone. Thisreconstruction starts with sending a patient to a radiologist forscanning, e.g. for a scan that generates medical volumetric data, suchas a CT, MRI scan or the like. The output of the scan can be a stack oftwo-dimensional (2D) slices forming a 3D data set. The output of thescan can be digitally imported into a computer program and may beconverted using algorithms known in the field of image processingtechnology to produce a 3D computer model of a relevant bone.Preferably, a virtual 3D model is constructed from the dataset using acomputer program such as Mimics™ as supplied by Materialise N.V.,Leuven, Belgium. Computer algorithm parameters are based on accuracystudies, as for instance described by Gelaude at al. (2008; Accuracyassessment of CT-based outer surface femur meshes Comput. Aided Surg.13(4): 188-199). A more detailed description for making a perfectedmodel is disclosed in U.S. Pat. No. 5,768,134 entitled ‘Method formaking a perfected medical model on the basis of digital imageinformation of a part of the body’.

Once the 3D volume of the bone is reconstructed, the surgeon (or personskilled in the art) can define the position of the implant and thepreferred position, orientation, depth and diameter of the screwtrajectories using a planning which can be used to fix the implant tothe bone. In non-limiting embodiments of the methods for manufacturingcustomized surgical guides according to the invention, the locationsand/or directions of the one or more screw insertions are determinedusing a planning procedure, which is performed pre-operatively.Alternatively, a planning procedure in the methods for manufacturing theguides may be performed during the operation/surgery, without havingperformed a pre-operative planning step. The planning of the surgicalintervention is done using suitable dedicated software, based onsuitable medical images (of which CT, MRI, are examples), taking intoaccount factors like bone quality and proximity to nerve bundles/bloodvessels or other anatomically sensitive objects. To plan and simulatethe intervention, images are imported into a computer workstationrunning 3D software. These images are manipulated as 3D surface meshes.The result is a computer simulation of the intervention, which outputs aplanning containing the information necessary for adapting theorientation of the guiding elements.

In specific embodiments of the methods for manufacturing the customizedsurgical guides according to the present invention, the step ofdetermining one or more screw trajectories comprises taking into accountone or more of the following criteria:

-   -   obtaining an optimal number of non-intersecting drill directions        for screw trajectories;    -   ensuring that the screw trajectories run through bone volume        with the optimal available quality;    -   ensuring optimal screw trajectory length; and    -   ensuring that the surrounding healthy soft tissue is optimally        preserved.

Accordingly, the step of determining one or more screw trajectories maycomprise obtaining an optimal number of non-intersecting drilldirections for screw trajectories. In order to obtain an optimal (whichmay imply a maximal) number of non-intersecting screw trajectories, aplanning is performed by analyzing the bone and the patient-specificimplant geometry. As a result, all of the screws for which screw holeswere foreseen in the planning, can be placed during surgery. The numberof screws is limited to the number actually useful. Foreseeing morescrew holes than necessary would weaken the implant in view of long-termfatigue, and would enlarge the size of the implant. The latter wouldimply unnecessary sacrificing of healthy neighbouring soft tissues.

The step of determining one or more screw trajectories may furthercomprise ensuring that the screw trajectories run through bone volumewith the optimal (which may imply the best) available quality. Thereto,planning is performed by analyzing the bone and patient-specific implantgeometry, and the grey values retrieved from the medical images. As aresult, screws are surrounded with bone with optimal traction strength.

In addition, the step of determining one or more screw trajectories mayfurther comprise ensuring that an optimal (which may imply a maximal)screw trajectory length is established. Thereto, planning is performedby analyzing the bone and patient-specific implant geometry, andpresence of implant components from foregoing surgeries which remain inplace. As a result, screws have a practical and sufficient length inorder to be useful and effective.

Finally, the step of determining one or more screw trajectories mayfurther comprise ensuring that the surrounding healthy soft tissue isoptimally (which may imply maximally) preserved. Thereto, a planning isperformed by analyzing the soft tissue.

The process of locating screws directly relates to determining theextent of the surface of the patient-specific implant covering the bonethrough which the screws will be inserted. In view of postoperativerestoration of patient functionality, screws protruding in—or implantportions overlaying—(healthy) soft tissues should be avoided as much aspossible, as in the case of muscle attachments, or is simply impossible,as in the case of nerves and blood vessels.

The foregoing criteria for adequately determining one or more screwtrajectories can be applied separately or, alternatively, can becombined. For example, the criterion of ensuring that the screwtrajectories run through bone volume with the optimal available qualityand the criterion of ensuring that an optimal (which may imply amaximal) screw trajectory length is established may be combined,resulting in the finding that screw trajectories which run through bonevolume with good bone quality but which are only small in length (i.e.small bone depth), are useless. For instance, in normal patients thecenter of the iliac wing consists of a double layer of strong corticalbone, though the trajectory length that can be established measures lessthan about 2 mm and therefore renders this location impractical forpositioning screws.

Also, the criterion of ensuring that the screw trajectories run throughbone volume with the optimal (which may imply the best) availablequality can be combined with the criterion of ensuring that an optimal(which may imply a maximal) screw trajectory length is established aswell as with the criterion of ensuring that the surrounding healthy softtissue is optimally preserved. For example, in determining the surfaceof the patient-specific acetabular implant covering the ilium, overlapwith the gluteus medius muscle is preferably avoided.

In addition, during the planning of determining one or more screwtrajectories the criterion of obtaining an optimal number ofnon-intersecting drill directions for screw trajectories may be combinedwith the criterion of ensuring that the screw trajectories run throughbone volume with the optimal available quality as well as with thecriterion of ensuring that an optimal (which may imply a maximal) screwtrajectory length is established and with the criterion of ensuring thatthe surrounding healthy soft tissue is optimally preserved.

Having defined the preferred position, orientation, depth and diameterof the screw trajectories, this information can be used to design thecustomized surgical guide that fits perfectly when placed on theimplant.

Designing a customized surgical guide according to the invention suchthat it fits on a patient-specific bone implant, comprises ensuring thatthe guiding elements are positioned corresponding to the pre-determinedscrew insertions. In particular embodiments, this further comprisesensuring, that one or more surface structures provide a supportivestructure connecting the one or more guiding elements and fit uniquely(and, where appropriate, specifically) on corresponding surfaces of thepatient-specific bone implant. Additionally or alternatively, the methodfurther comprises ensuring hat one or more locking features fit on theimplant in a unique way.

A preferred method for designing the surgical template uses a computerprogram such as 3-matic™ as supplied by Materialise N.V., Leuven,Belgium. Alternatively, the surgical guide is automatically generatedbased on the information of preferred position, orientation, depth anddiameter of the screw trajectories. In a particular non-limitingembodiment, this method uses a number of design parameters as an inputincluding, but not limited to, the dimensions of the surgical tools asused by the medical practitioner, the contact area of the surgical guidewith the patient-specific implant at the positions where the surgicaltool is to be placed, etc.

More particularly the step of producing the customized surgical guideaccording to the invention implies producing and assembling thedifferent parts thereof, i.e. producing one or more surface structures(as described herein), one or more guiding elements (as describedherein), and optionally one or more connecting structures (as describedherein), which interconnect the different parts of the guiding tool.

More particularly, the step of producing the customized surgical guideaccording to the invention implies positioning the one or more guidingelements (as described herein), and optionally the one or more surfacestructures (as described herein), the one or more connecting structures(as described herein) and/or the one or more locking features such thatthe guide fits perfectly and uniquely (i.e. only in that position) ontothe patient-specific implant. The one or more surface structures of thecustomized surgical guides according to the present invention may bepositioned such that they may serve as a base or supportive structurefor the one or more guiding elements of the guides and additionally oralternatively, that they may ensure the unique (and optionally,specific) fit of the surgical guides with the patient-specific implant.Indeed, where the outer surface (i.e. the surface opposite of thesurface facing the bone) of the patient-specific implant corresponds toa standard shape (or one of a selection of standard shapes), the one ormore surfaces are designed to ensure or to be able to ensure a “singlefit” (i.e. only one position fits) with all implants having the samestandard outer surface. Where the outer surface or external morphologyof the patient-specific implant is also specific to the implant, thesespecific features may ensure a unique fit (i.e. only one position fitsand only there is an optimal fit only on the corresponding implant andpatient on which it is based) of the customized guide on to thepatient-specific implant.

The position of the one or more guiding elements comprised in thesurgical guides is determined by the planned direction of a surgicalinstrument into the bone or joint. As determined by the nature of theimplant, the guiding elements can be positioned on the one or moresurface structures and/or on the one or more connecting structures. Theposition of the one or more connecting structures of the customizedsurgical guides according to the invention is preferably such that itprovides, in addition to a connection between the one or more surfacestructures and the one or more guiding elements, a base or supportivestructure for one or more guiding elements, and/or additionally oralternatively, a contribution to the specific fit with thepatient-specific implant.

In particular embodiments, the customized surgical guides according tothe invention are prepared by rapid manufacturing techniques, alsoreferred to as layered manufacturing techniques or material depositionmanufacturing techniques.

Rapid manufacturing includes all techniques whereby an object is builtlayer by layer or point per point by adding or hardening material (alsocalled free-form manufacturing). The best known techniques of this typeare stereolithography and related techniques, whereby for example abasin with liquid synthetic material is selectively cured layer by layerby means of a computer-controlled electromagnetic beam; selective lasersintering, whereby powder particles are sintered by means of anelectromagnetic beam or are welded together according to a specificpattern; fused deposition modeling, whereby a synthetic material isfused and is stacked according to a line pattern; laminated objectmanufacturing, whereby layers of adhesive-coated paper, plastic, ormetal laminates are successively glued together and cut to shape with aknife or laser cutter; or electron beam melting, whereby metal powder ismelted layer per layer with an electron beam in a high vacuum.

In particular embodiments, Rapid Prototyping and Manufacturing (RP&M)techniques, are used for manufacturing the customized surgical guides ofthe invention. Rapid Prototyping and Manufacturing (RP&M) can be definedas a group of techniques used to quickly fabricate a physical model ofan object typically using three-dimensional (3-D) computer aided design(CAD) data of the object. Currently, a multitude of Rapid Prototypingtechniques is available, including stereo lithography (SLA), SelectiveLaser Sintering (SLS), Fused Deposition Modeling (FDM), foil-basedtechniques, etc.

A common feature of these techniques is that objects are typically builtlayer by layer. Stereo lithography, presently the most common RP&Mtechnique, utilizes a vat of liquid photopolymer “resin” to build anobject a layer at a time. On each layer, an electromagnetic ray, e.g.one or several laser beams which are computer-controlled, traces aspecific pattern on the surface of the liquid resin that is defined bythe two-dimensional cross-sections of the object to be formed. Exposureto the electromagnetic ray cures, or, solidifies the pattern traced onthe resin and adheres it to the layer below. After a coat had beenpolymerized, the platform descends by a single layer thickness and asubsequent layer pattern is traced, adhering to the previous layer. Acomplete 3-D object is formed by this process.

Selective laser sintering (SLS) uses a high power laser or anotherfocused heat source to sinter or weld small particles of plastic, metal,or ceramic powders into a mass representing the 3-dimensional object tobe formed.

Fused deposition modeling (FDM) and related techniques make use of atemporary transition from a solid material to a liquid state, usuallydue to heating. The material is driven through an extrusion nozzle in acontrolled way and deposited in the required place as described amongothers in U.S. Pat. No. 5,141,680.

Foil-based techniques fix coats to one another by means of gluing orphoto polymerization or other techniques and cut the object from thesecoats or polymerize the object. Such a technique is described in U.S.Pat. No. 5,192,539.

Typically RP&M techniques start from a digital representation of the 3-Dobject to be formed. Generally, the digital representation is slicedinto a series of cross-sectional layers which can be overlaid to formthe object as a whole. The RP&M apparatus uses this data for buildingthe object on a layer-by-layer basis. The cross-sectional datarepresenting the layer data of the 3-D object may be generated using acomputer system and computer aided design and manufacturing (CAD/CAM)software.

A selective laser sintering (SLS) apparatus is in particular embodimentsused for the manufacture of the customized surgical tool from a computermodel. It should be understood however, that various types of rapidmanufacturing and tooling may be used for accurately fabricating thesecustomized surgical guides including, but not limited to,stereolithography (SLA), Fused Deposition Modeling (FDM) or milling.Also, while rapid prototypic methods are particularly useful in thecontext of the present inventions, the guides according to the presentinvention can similarly be manufactured using other methods.

The surgical guides of the invention may be manufactured in differentmaterials. Typically, only materials that are biocompatible (e.g. USPclass VI compatible) with the human body are taken into account.Preferably the customized surgical guide is formed from a heat-tolerablematerial allowing it to tolerate high-temperature sterilization. In thecase SLS is used as a RP&M technique, the surgical template may befabricated from a polyamide such as PA 2200 as supplied by EOS, Munich,Germany or any other material known by those skilled in the art may alsobe used.

The invention further provides computer programs for performing themanufacturing methods of the present invention. More particularly, thepresent invention provides computer program products for enabling adevice to execute at least part of the methods according to theinvention described herein.

In particular embodiments, computer programs are provided for providinga design of a customized surgical guide comprising one or more customguiding elements and/or one or more customized surface structures basedon (1) one or more images of the bone and the patient-specific boneimplant thereon; and (2) one or more screw trajectories determined bypre-operative planning, respectively. In particular embodiments, the oneor more guiding elements of the guide are positioned corresponding tothe pre-operatively planned screw insertions. Additionally oralternatively, the one or more customized surface structures of theguide are designed to ensure a unique fit between the patient-specificbone implant and the guide by way of a congruency or complementaritybetween the customized surface structure(s) and the patient-specificmorphology of the patient-specific bone implant. Additionally oralternatively, the one or more locking features of the guide aredesigned to ensure a unique fit between the patient-specific boneimplant and the guide by way of a congruency or complementarity betweenthe locking feature(s) the patient-specific bone implant.

In further particular embodiments the computer programs further ensurethe production of the surgical guide according to the invention by anadditive manufacturing device. Suitable devices for manufacturing theguides according to the present invention are known to the skilledperson and detailed hereinabove.

Yet a further aspect of the invention relates to the use of thecustomized surgical guides described herein to ensure stable fixation ofa patient-specific implant. According to this aspect, the presentinvention provides methods for fixing a patient-specific bone implantonto a bone, which in particular embodiments comprises the steps of:

-   (a) placing a customized surgical guide according to the invention    onto a patient-specific bone implant provided in the body;-   (b) introducing the screw trajectories with the appropriate surgical    tools;-   (c) removing said customized surgical guide; and (optionally)-   (d) fixing the patient-specific bone implant with screws onto the    bone.

In particular embodiments, e.g. where self-tapering screws are used, thescrew trajectories are established upon introduction of the screws instep (b). This may ensure the fixing of the implant onto the bone, suchthat step (d) is no longer or only partially required. In furtherparticular embodiments, combinations of fastening tools are used

More particularly, the step of placing a customized surgical guideaccording to the invention onto a patient-specific bone implant impliesthat the customized surgical guide is placed onto the patient-specificbone or joint implant such that it fits, mates, coincides and/or engageswith the (specific) features of the patient-specific implant. This mayinvolve ensuring that the one or more customized surface structuresadequately mate with the corresponding surfaces on the implant and/orensuring that the locking features on the customized surgical guide fiton the implant.

The methods according to this aspect of the invention further comprisethe step of introducing the different screw trajectories with theappropriate surgical tools. As described above this includes but is notlimited to a pre-drill, drill, a saw, jig saw, mill or lateral drill andfastening tools such as screw. Based on the position of the guides (andoptionally the stops provided therein) an appropriate screw trajectoryis provided.

The methods for fixing the patient-specific bone implant onto a boneaccording to the invention further comprise the step of removing thecustomized surgical guide. This step can be performed either before orafter the implant has been fixed to the bone. According to particularembodiments, after the screw trajectories have been introduced, thesurgical guide is removed in order to allow final fixation of thepatient-specific implant onto the bone or joint. Alternatively, theimplant is fixed to the bone first and the guide is removed thereafter.The methods of the present invention have the advantage that thepatient-specific implant is already in place within the sometimes verynarrow and deep surgical window, is maintained during introduction ofthe screw trajectories, and does not need to be removed prior tofixation.

Accordingly, the methods for fixing the patient-specific bone implantonto a bone further comprise, either before or after removal of thecustomized surgical guide, the step of (partly) fixing thepatient-specific bone implant with screws onto the bone or joint. Toolsfor performing fixation with screws are known to the person skilled inthe art.

EXAMPLES

The invention is further illustrated herein below by means of thefollowing non-limiting embodiments.

In particular embodiments, the invention is applied for acetabular cupreplacement and the custom surgical guides according to the presentinvention are designed to fit on a patient-specific acetabular implant.

According to particular embodiments, the connecting structure may be aring structure and one or more surface structures are designed to fitonto one or more surfaces of the patient-specific acetabular implant.For instance, in these embodiments, the one or more surfaces of thepatient-specific acetabular implant may be designed based on specificanatomic features of one or more of the ilium, ischium and/or pubis ofthe hip joint.

In particular embodiments, the present invention provides customizedsurgical guides for a patient-specific acetabular implant comprising oneor more surface structures, and one or more guiding elements, wherein atleast one of said one or more surface structures is designed to fit onthe patient-specific acetabular implant. The acetabulum is thecup-shaped joint socket of the hip wherein the femur head articulates.In general, a joint prosthesis consists of a convex component thatarticulates in a concave socket, such as for instance in hip jointarthroplasty, a femoral head is mounted on a stem articulating in anacetabular cup. The following paragraph further describes the inventionby means of the specific embodiment of a customized surgical guide for apatient-specific acetabular implant as illustrated in FIGS. 1 to 3.

The patient-specific acetabular implant according to the embodimentdescribed herein comprises a hemispherical cup, which is rigidlyconnected to the host bone with projected patient-specific surfaces thatprovide intimate contact between the implant and the ilial, ischial andpubic host bones. FIG. 2A represents a severe acetabular defect of theleft hemi-pelvis (1), which is to be treated with a patient-specificacetabular implant (2). A customized guide (3) according to the presentinvention as represented in FIGS. 1, 2C, 2D and 2E and 3 is designedthat fits on the implant (2) to guide the planned drill directions (4)for the screws which will be inserted in a planned direction through theimplant screw holes (12). The customized surgical guide (3) for apatient-specific acetabular implant consists of a central ring structure(5) mating with the acetabular rim (13) of the acetabular implant (2) asshown in FIGS. 2B, 2C and 2D. The customized surgical guide for theacetabular implant according to the present embodiment comprises one ormore surface structures (7), (8) and (9), which comprise at least oneimplant-specific area of the external morphology by which the correctplacement of the guide on the patient-specific implant is ensured. Asshown in FIGS. 1 and 3, the one or more of the surface structures (7),(8), and (9) extend from the central ring (5) and comprise the one ormore implant-specific areas, which are fully complementary topatient-specific areas (17), (18) and (19) of the external morphology ofthe acetabular implant. The side of each of these three surfacestructures which faces the bone is specifically designed to fit onanatomical features of each of the ilium, ischium and pubis,respectively. As presented in FIG. 2B, the patient-specific areas of theexternal morphology (17), (18) and (19) of the acetabular implant (2)comprise one or more screw holes (12). The one or more locking features(6) on the central ring (5), as presented in FIGS. 1 and 2D, addtranslational stability by preventing slide-off of the customized guide(3) in the plane of the acetabular rim (13). These locking features (6)still allow application of the customized guide (3) onto thepatient-specific implant (2). Rotational stability, either uni- orbi-directionally, results primarily from the unique curvature fit of thecontact area between the one or more surface structures (7), (8), and(9) and the patient-specific implant (2). Rotational stability can befurther improved by adding locking features positioned on the surfacestructures (7), (8), and (9) of the customized guide, which mate withcorresponding locking features present in the patient-specific implant(2). FIGS. 1 and 3 show cylindrical drill guiding elements (10) that arepositioned on the surface structures of the customized guide (3)according to this specific embodiment to guide the insertion of a screwpre-drill instrument at the location of the implant screw holes (12)present in the surface structures (7), (8), and (9). In this specificembodiment, the pre-drilled screw holes are meant/suitable for corticalscrews. Furthermore, additional (cylindrical drill) guiding elements(11) (shown in FIG. 3) are positioned on or within the cavity formed bythe acetabular portion (14) (shown in FIG. 2B) of the patient-specificimplant (2), being attached by bridging structures (21) (shown in FIG.3) to the central ring (5), to guide the insertion of a screw pre-drillinstrument at the location of the implant screw holes present in theacetabular portion (14). In this specific embodiment, the pre-drilledscrew holes are meant/suitable for trabecular screws. In someembodiments, a portion of the drill guiding elements (11) may bepositioned below the level of the plane formed by the acetabular rim(13) of the patient-specific implant (2). In general, cylindrical drillguiding elements (10) and (11) can be mutually intersecting to provideguidance and allow drilling within the available working space. In thepresent example this is the case for the cylindrical drill guidingelement (11) in the cavity formed by the acetabular portion (14) of theimplant (2), in order to enable drilling from within the availablesurgical window.

The diameter of cylindrical drill guiding elements (10) and (11) isdetermined based on the diameter of the pre-drill instrument, while theheight is determined to provide sufficient stability and/or guidance ofthe same instrument. The cylindrical drill guiding elements (10) and(11) can also be trimmed either straight, obliquely, or with a complexlyshaped cut in order to fit the surgical window. To solve visualorientation problems in case of obliquely trimmed cylinders, adisc-shaped visual reference ring (20), as shown in FIG. 2E, can beadded at the base of the drill guiding cylinders (10) and (11) toprovide visual feedback to the surgeon. The plane normal of the disc(20) equals the planned drill direction (4). As an additional oralternative visual reference, a wing element (22) as for example shownin FIG. 5, can be provided in case of drill guiding elements withoverlying soft tissue. The wing is for example attached to a drillguiding element (10) or (11), or at some other location of thecustomized guide (3). The wing element provides visual feedback to thesurgeon, minimizing potential misinterpretation resulting from obscuredanatomical reference points, or potentially confusing orientations ofthe surface structures (7), (8) and (9) of the customized guide (3).

In the present embodiment, a cylindrical drill guiding element can behalved lengthwise, as illustrated by the halved cylindrical drillguiding element (23) in FIG. 6, allowing (partial) insertion of a screwdirectly in the implant, and subsequent removal of the customized guidewith the inserted screw left in place. Doing so reduces degrees offreedom of the patient-specific implant (2) and customized guide (3)during drilling, and assures that correspondence between pre-drills andscrew holes is not lost. In the present embodiment, the cylindricalguiding elements (10) and (11) may comprise an extension (16), shown inFIG. 4, into the implant screw hole, while still allowing insertion ofthe pre-drill instrument. Doing so reduces the degrees of freedom of thecustomized guide (3) relatively to the patient-specific implant (2).This is an example of an additional locking feature between guide andimplant.

In particular embodiments, the present application provides incustomized surgical guides for a patient-specific acetabular implantcomprising one or more guiding elements, wherein one or more of theguiding elements are provided with a locking feature. In suchembodiments, the locking feature may comprise an extension of theguiding element which fits into a screw hole of the implant. Thefollowing paragraph further describes the invention by means of thespecific embodiment of a customized surgical guide for apatient-specific acetabular implant (25) as illustrated in FIG. 9.

The patient-specific acetabular implant (25) comprises a hemisphericalcup, which fits the patient's (reamed) acetabulum. The cup is providedwith a plurality of screw holes (12), and may further be provided with aporous osteoconductive scaffold to promote the attachment of the implantto the bone. Unlike the implant (2) as illustrated in FIG. 2B, theimplant (25) of FIG. 9 is not provided with projected patient-specificsurfaces for contacting the ilial, ischial and pubic host bones.Typically, implant (25) is used for less severe bone defects thanimplant (2).

A particular embodiment of a customized guide (26) as described hereinis represented in FIGS. 8 to 10. The guide (26) is designed such that itfits on the implant (25) to guide the planned drill directions for thescrews which will be inserted in a planned direction through the implantscrew holes (12).

More particularly, the guide (26) is provided with a plurality ofguiding elements, more particularly drill cylinders (27). Each of thedrill cylinders is provided with a locking feature (16), which forms anextension of the corresponding drill cylinder and fits into one of thescrew holes (12) of the implant, for example as shown in FIG. 4. Aunique and (rotationally and translationally) stable fit of the guide(26) on the implant (25) can be achieved by positioning the lockingfeatures (16) of the guiding instrument into the screw holes (12) of theimplant. The position and direction of the drill cylinders (27) andlocking features (16) on the guide (26) is such that when the guide ispositioned on the implant (25) via the locking features, the drillcylinders (27) guide the planned drill directions for the screws whichwill be inserted through the implant screw holes. The guide (26) mayfurther be provided with a surface structure (28) which is complementaryto a part of the cavity (14) formed by the acetabular implant (26), forproviding additional stability. The surface structure (28) furtherensures that all locking features (16) and drill cylinders (27) arerigidly interconnected.

In certain embodiments, the surgical guides described herein maycomprise one or more locking features which are not associated with oneof the guiding elements. As described above, such locking features mayfit onto corresponding locking features present in the patient-specificimplant. However, the presence of such corresponding locking features onthe implant is not critical. For example, the locking features maycomprise an extension of the guiding element which fits onto a lateralpart of a patient-specific surface of the implant, as shown in FIGS. 11and 12.

FIGS. 11A and 11B show a particular embodiment of a surgical guide (31)as described herein, positioned on an implant (30) which is itselfpositioned on a pelvic bone (25). The implant (31) as such is shown inFIG. 13 and is similar to the implant (2) of FIG. 2B. FIG. 12 shows thesurgical guide (31) as such.

The exemplified guide combines different optional features of the guidesenvisaged herein. The illustrated guide (31) has features which aresimilar in form and function to the features of the guide (3) shown inFIG. 1. More particularly, the guide (31) comprises a central ringstructure (5) mating with the acetabular rim of the implant (30). Thoughnot critical to all aspects of the guides envisaged herein, the guidemay further comprise one or more surface structures (7), (8) and (9),which can comprise an implant-specific area of the external morphologyby which the correct placement of the guide on the patient-specificimplant is ensured. In these embodiments, upon use, the surfacestructures (7), (8) and (9) are positioned on the patient-specificsurfaces (17), (18) and (19) of the implant (30), respectively, therebyproviding a unique fit.

Additionally or alternatively, one or more locking features (6) on thecentral ring (5) ensures translational stability by preventing slide-offof the customized guide (31) in the plane of the acetabular rim (13).Bi-directional rotational stability is provided by locking features (32)which laterally engage with protrusions the implant (30). Suchprotrusions can, for instance, be part of the lateral flanges (18) and(19) of the implant. The locking features (32) in this embodiment formextensions of the central ring structure (5) and each comprise a surfacematching an edge of the surface structure of the implant (30). Thisensures a unique fit of the guide on the implant. In particularembodiments such as the one illustrated in FIGS. 11 and 12, rotationaland translational stability may also (additionally or alternatively) beensured by the unique curvature fit of the contact area between the oneor more surface structures (7), (8), and (9) and the external surface ofthe patient-specific implant (2).

The guide (31) further comprises drill guiding elements (10) positionedon the surface structures of the customized guide (31), and drillguiding elements (11) positioned on or within the cavity formed by theacetabular portion of the patient-specific implant (30). The latterguiding elements (11) can guide the insertion of a screw pre-drillinstrument at the location of the implant screw holes present in theacetabular portion of the implant (30) and are attached by bridgingstructures (21) to the central ring (5). Optionally, one or more of theguiding elements (10) and/or (11) may be provided with a locking featurewhich forms an extension of the corresponding drill cylinder and fitsinto one of the screw holes of the implant, as described above.

1. A combination of a patient-specific bone implant; and a customizedsurgical guide for surgical instruments for placement on saidpatient-specific bone implant, said customized surgical guide comprisingone or more customized guiding elements; and at least one lockingfeature which can interlock with said implant; wherein said customizedsurgical guide and said bone implant engage by means of a unique fit,ensured by the position and orientation of said locking feature.
 2. Thecombination according to claim 1, wherein said patient-specific boneimplant is provided with a hole and said locking feature fits into saidhole.
 3. The combination according to claim 1, wherein said lockingfeature forms an extension of one of said guiding elements.
 4. Thecombination according to claim 1, wherein said implant has an externalmorphology, and wherein said customized surgical guide further comprisesa surface structure extending over at least part of said externalmorphology.
 5. The combination according to claim 4, wherein saidlocking feature is provided on said surface structure.
 6. Thecombination according to claim 1, wherein said bone implant is apatient-specific bone prosthesis.
 7. The combination according to claim1, wherein said bone implant is a patient-specific acetabular implant.8. The combination according to claim 1, wherein said one or moreguiding elements include drill guiding elements.
 9. The combinationaccording to claim 8, wherein said one or more drill guiding elementsfurther comprise a drill stop.
 10. The combination according to claim 1,wherein said one or more guiding elements include cutting guidingelements.
 11. The combination according to claim 10, wherein said one ormore cutting guiding elements further comprise a cutting stop.
 12. Thecombination according to claim 1, wherein said customized surgical guidefurther comprises an element serving as a visual reference forperforming a surgical interaction.
 13. A customized surgical guide forsurgical instruments for placement on a patient-specific bone implant,said customized surgical guide comprising: one or more customizedguiding elements; and at least one locking feature; wherein saidcustomized surgical guide and said bone implant engage by means of aunique fit, ensured by the position and orientation of said lockingfeature.
 14. The customized surgical guide according to claim 13,wherein said locking feature forms an extension of one of said guidingelements.
 15. A method for producing a customized surgical guide forsurgical instruments for placement on a patient-specific bone implant,comprising the steps of: (a) designing, based on an image the bone andthe patient-specific bone implant thereon; and one or more screwinsertions determined by pre-operative planning, a customized surgicalguide comprising one or more custom guiding elements, one or moresurface structures extending over at least part of the surface of thepatient-specific bone implant; and optionally a connecting structure,connecting said customized guiding elements and said one or more surfacestructures at least one locking feature and (b) producing saidcustomized surgical guide based on the design obtained in step (a),wherein: the one or more guiding elements of said guide are positionedcorresponding to said one or more pre-operatively planned screwinsertions; and the one or more locking features of said guide ensure aspecific interlock of the customized surgical guide with thepatient-specific implant thereby ensuring a unique fit between thepatient-specific bone implant and said guide.
 16. The method accordingto claim 15, wherein said patient-specific bone implant is provided witha hole and said locking feature fits into said hole.
 17. The methodaccording to claim 16, wherein said one or more locking features form anextension of said one or more guiding elements and fit into a hole ofsaid implant corresponding to said screw trajectory.
 18. The method ofclaim 15, wherein said step of determining one or more screwtrajectories using a planning comprises taking into account one or moreof the following criteria: obtaining an optimal number ofnon-intersecting drill directions for screw trajectories; ensuring thatsaid screw trajectories run through bone volume with the optimalavailable quality; ensuring optimal screw trajectory length; andensuring that the surrounding healthy soft tissue is optimallypreserved.
 19. The method according to claim 15, wherein said customizedsurgical guide is made by additive manufacturing.
 20. A method forfixing a patient-specific bone implant onto a bone, comprising the stepsof: (a) placing a customized surgical guide according to claim 1 onto apatient-specific bone implant according to claim 1; wherein a unique fitof said customized surgical guide on said patient-specific bone implantis ensured by the fitting of said locking features of said guide; (b)introducing the screw trajectories in the implant with the appropriatesurgical tools; (c) removing said customized surgical guide; and (d)fixing the patient-specific bone implant with one or more screws ontothe bone; wherein step (d) in said method can be either prior to orafter step (c), or both.